Drug Information

Product NDC: 63629-4872

Proprietary Name: Lamivudine and Zidovudine

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Bryant Ranch Prepack
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/15/2012

Package Information

No. Package Code Package Description Billing Unit
163629-4872-16 TABLET, FILM COATED in 1 BOTTLE (63629-4872-1)
263629-4872-260 TABLET, FILM COATED in 1 BOTTLE (63629-4872-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC63629-4872The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMELamivudine and ZidovudineThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/15/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEBryant Ranch PrepackName of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 7/3/2020